Altered Bone Status in Rett Syndrome

Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-linked MECP2 gene, encoding for methyl-CpG binding protein 2 (MeCP2), a multifaceted modulator of gene expression and chromatin organization. Based on the type of mutation, RTT patients exhibit a broad...

Descripción completa

Detalles Bibliográficos
Autores principales: Pecorelli, Alessandra, Cordone, Valeria, Schiavone, Maria Lucia, Caffarelli, Carla, Cervellati, Carlo, Cerbone, Gaetana, Gonnelli, Stefano, Hayek, Joussef, Valacchi, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230033/
https://www.ncbi.nlm.nih.gov/pubmed/34205017
http://dx.doi.org/10.3390/life11060521

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230033/
https://www.ncbi.nlm.nih.gov/pubmed/34205017
http://dx.doi.org/10.3390/life11060521

Ejemplares similares